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2-(2-phenylethylsulfanyl)ethanol

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Identification
Molecular formula
C10H14OS
CAS number
16239-55-1
IUPAC name
2-(2-phenylethylsulfanyl)ethanol
State
State

At room temperature, 2-(2-phenylethylsulfanyl)ethanol is in a liquid state. It is typically utilized and stored as a liquid under standard laboratory conditions.

Melting point (Celsius)
29.00
Melting point (Kelvin)
302.15
Boiling point (Celsius)
302.20
Boiling point (Kelvin)
575.35
General information
Molecular weight
184.29g/mol
Molar mass
184.2930g/mol
Density
1.0860g/cm3
Appearence

2-(2-phenylethylsulfanyl)ethanol is a colorless to pale yellow liquid. It has a characteristic aromatic odor attributable to its phenyl group structure. The compound is typically clear and may become more viscous at lower temperatures.

Comment on solubility

Solubility of 2-(2-phenylethylsulfanyl)ethanol

The solubility of 2-(2-phenylethylsulfanyl)ethanol is an interesting topic due to its unique structure, which influences its interaction with various solvents. Generally, this compound is expected to be:

  • Moderately soluble in polar solvents: Compounds with hydroxyl (-OH) groups tend to engage in hydrogen bonding, often leading to increased solubility in water and alcohols.
  • Less soluble in non-polar solvents: As the bulkiness of the phenyl group increases the hydrophobic character of the molecule, solubility might diminish in organic solvents that lack polarity.

When considering its solubility, it can be useful to remember the maxim: "Like dissolves like." Thus, the polar nature of the hydroxyl group likely facilitates the compound's ability to dissolve in similar polar environments. However, the presence of the phenylethylsulfanyl group introduces some degree of hydrophobicity, which could complicate solubility in purely aqueous contexts.

To summarize, the solubility of 2-(2-phenylethylsulfanyl)ethanol is characterized by:

  1. High solubility in polar solvents such as water and alcohols.
  2. Decreased solubility in non-polar solvents.

The balance between its polar and non-polar characteristics makes it a fascinating compound to explore in terms of solubility behavior!

Interesting facts

Interesting Facts about 2-(2-phenylethylsulfanyl)ethanol

2-(2-phenylethylsulfanyl)ethanol is a fascinating compound with unique characteristics and applications that make it noteworthy within the field of chemistry. Here are some intriguing facts about this compound:

  • Structure Diversity: This compound features a sulfanyl (–SH) group attached to a phenyl-ethyl moiety. This diverse structure contributes to its reactivity and interaction with various biological systems.
  • Biological Relevance: Compounds with sulfanyl groups often exhibit interesting biological properties. They can act as antioxidants, and there's research exploring their potential uses in medicinal chemistry.
  • Flavor and Fragrance: Substituted alcohols, like 2-(2-phenylethylsulfanyl)ethanol, are sometimes used in formulations for flavors and fragrances. The presence of the phenyl group may lend aromatic qualities beneficial for these applications.
  • Reaction Potential: The sulfanyl group makes this compound a potential candidate for a variety of chemical reactions. Its ability to form thiol derivatives can be harnessed in synthetic chemistry to create novel compounds.
  • Research Insights: This compound can provide insights into the mechanisms of sulfide functionalities in organic compounds and opens up avenues for further research in organosulfur chemistry.

In summary, 2-(2-phenylethylsulfanyl)ethanol is more than just a chemical name; it embodies a rich tapestry of chemical interactions and potential applications. As the study of organosulfur compounds progresses, we may uncover even more about the roles these types of molecules can play in both nature and synthetic chemistry.

Synonyms
ETHANOL, 2-(PHENETHYLTHIO)-
3778-82-3
BRN 3239580
2-(beta-Phenylethylthio)ethanol
4-06-00-03086 (Beilstein Handbook Reference)
2-(2-Phenylethylthio)ethanol
SCHEMBL9180229
2-[(2-Phenylethyl)thio]ethanol
DTXSID40191224
KGZHEXGRHGYQNI-UHFFFAOYSA-N